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Sui-Fan Tong

Showing results (11-20 of 26) with videos related to

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Molecular Genetics and Metabolism|November 1, 2002
Novel missense mutation (Y24H) in the G6PT1 gene causing glycogen storage disease type 1bYuet-Ping Yuen, Wai-Fun Cheng, Sui-Fan Tong, et al.
The Journal of Investigative Dermatology|January 19, 2005
DNA-based diagnosis of xeroderma pigmentosum group C by Whole-genome scan using single-nucleotide polymorphism microarrayChing-Wan Lam, Kitty Kit-Ting Cheung, Nai-Ming Luk, et al.
Journal of Hepatology|November 18, 2005
A patient with novel ABCB11 gene mutations with phenotypic transition between BRIC2 and PFIC2Ching-Wan Lam, Ka-Ming Cheung, Man-Shan Tsui, et al.
Clinica Chimica Acta; International Journal of Clinical Chemistry|June 21, 2005
Novel missense mutation in the CASR gene in a Chinese family with familial hypocalciuric hypercalcemiaChing-Wan Lam, Ka-Fai Lee, Angel On-Kei Chan, et al.
Journal of Human Genetics|October 13, 2006
DNA-based diagnosis of malignant osteopetrosis by whole-genome scan using a single-nucleotide polymorphism microarray: standardization of molecular investigations of genetic diseases due to consanguinityChing-Wan Lam, Sui-Fan Tong, Keong Wong, et al.
Sleep & Breathing = Schlaf & Atmung|August 12, 2009
Maternally inherited Leigh syndrome: an unusual cause of infantile apneaChristy Shuk-kuen Chau, Ka-li Kwok, Daniel K Ng, et al.
Chinese Medical Journal|July 23, 2002
Novel mitochondrial 16S rRNA mutation, 3200T-->C, associated with adult-onset type 2 diabetesTao Yang, Ching-Wan Lam, Man-Wo Tsang, et al.
Molecular Genetics and Metabolism|February 5, 2002
DNA-based diagnosis of isolated sulfite oxidase deficiency by denaturing high-performance liquid chromatographyChing-Wan Lam, Chi-Keung Li, Chi-Kong Lai, et al.
Molecular Genetics and Metabolism|August 15, 2002
Novel mutations in the PATCHED gene in basal cell nevus syndromeChing-Wan Lam, Chi-Yan Leung, Kam-Cheong Lee, et al.
Molecular Genetics and Metabolism|November 16, 2004
DNA-based subtyping of glycogen storage disease type III: mutation and haplotype analysis of the AGL gene in ChineseChing-Wan Lam, Allen Ting-Chun Lee, Yuen-Yu Lam, et al.
Pageof 3

Showing results (11-20 of 26) with videos related to

Sort By:
Pageof 3
Molecular Genetics and Metabolism|November 1, 2002
Novel missense mutation (Y24H) in the G6PT1 gene causing glycogen storage disease type 1bYuet-Ping Yuen, Wai-Fun Cheng, Sui-Fan Tong, et al.
The Journal of Investigative Dermatology|January 19, 2005
DNA-based diagnosis of xeroderma pigmentosum group C by Whole-genome scan using single-nucleotide polymorphism microarrayChing-Wan Lam, Kitty Kit-Ting Cheung, Nai-Ming Luk, et al.
Journal of Hepatology|November 18, 2005
A patient with novel ABCB11 gene mutations with phenotypic transition between BRIC2 and PFIC2Ching-Wan Lam, Ka-Ming Cheung, Man-Shan Tsui, et al.
Clinica Chimica Acta; International Journal of Clinical Chemistry|June 21, 2005
Novel missense mutation in the CASR gene in a Chinese family with familial hypocalciuric hypercalcemiaChing-Wan Lam, Ka-Fai Lee, Angel On-Kei Chan, et al.
Journal of Human Genetics|October 13, 2006
DNA-based diagnosis of malignant osteopetrosis by whole-genome scan using a single-nucleotide polymorphism microarray: standardization of molecular investigations of genetic diseases due to consanguinityChing-Wan Lam, Sui-Fan Tong, Keong Wong, et al.
Sleep & Breathing = Schlaf & Atmung|August 12, 2009
Maternally inherited Leigh syndrome: an unusual cause of infantile apneaChristy Shuk-kuen Chau, Ka-li Kwok, Daniel K Ng, et al.
Chinese Medical Journal|July 23, 2002
Novel mitochondrial 16S rRNA mutation, 3200T-->C, associated with adult-onset type 2 diabetesTao Yang, Ching-Wan Lam, Man-Wo Tsang, et al.
Molecular Genetics and Metabolism|February 5, 2002
DNA-based diagnosis of isolated sulfite oxidase deficiency by denaturing high-performance liquid chromatographyChing-Wan Lam, Chi-Keung Li, Chi-Kong Lai, et al.
Molecular Genetics and Metabolism|August 15, 2002
Novel mutations in the PATCHED gene in basal cell nevus syndromeChing-Wan Lam, Chi-Yan Leung, Kam-Cheong Lee, et al.
Molecular Genetics and Metabolism|November 16, 2004
DNA-based subtyping of glycogen storage disease type III: mutation and haplotype analysis of the AGL gene in ChineseChing-Wan Lam, Allen Ting-Chun Lee, Yuen-Yu Lam, et al.
Pageof 3